EP0884650A1 - Photosensitive recording material using microcapsules - Google Patents

Photosensitive recording material using microcapsules Download PDF

Info

Publication number
EP0884650A1
EP0884650A1 EP98304014A EP98304014A EP0884650A1 EP 0884650 A1 EP0884650 A1 EP 0884650A1 EP 98304014 A EP98304014 A EP 98304014A EP 98304014 A EP98304014 A EP 98304014A EP 0884650 A1 EP0884650 A1 EP 0884650A1
Authority
EP
European Patent Office
Prior art keywords
recording material
material according
dyes
methacrylate
acrylate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP98304014A
Other languages
German (de)
French (fr)
Inventor
Minobu c/o Brother Kogyo K.K. Maeda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Brother Industries Ltd
Original Assignee
Brother Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Brother Industries Ltd filed Critical Brother Industries Ltd
Publication of EP0884650A1 publication Critical patent/EP0884650A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004—Photosensitive materials
    • G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
    • G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
    • G03F7/029—Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/002—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor using materials containing microcapsules; Preparing or processing such materials, e.g. by pressure; Devices or apparatus specially designed therefor
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/002—Photosensitive materials containing microcapsules
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
    • Y10S430/1055—Radiation sensitive composition or product or process of making
    • Y10S430/114—Initiator containing
    • Y10S430/122—Sulfur compound containing
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
    • Y10S430/1055—Radiation sensitive composition or product or process of making
    • Y10S430/127—Spectral sensitizer containing

Definitions

  • the present invention relates to a photosensitive recording material using microcapsules, and in particular to a photosensitive recording material using microcapsules that contain core materials in a specific combination.
  • the microcapsules are commonly applied over the entire surface of the recording medium, the surface of the photosensitive recording material is exposed to form a latent image based on the image that is to be recorded, and the recording medium on which the latent image has been formed is pressurized to visualize and record the image.
  • the microcapsules harden in the portions that is exposed, but do not harden in the unexposed portions, and since the capsules themselves are not destroyed by pressure in the portions where the microcapsules have hardened, they do not colorize in the portions where they have hardened when the recording medium on which the latent image has been formed is pressurized by a pressurization device, while the microcapsules are destroyed according to the wavelength of the exposure light in the portions where the capsules have not hardened, resulting in the development of color by a coloring reaction.
  • microcapsules sometimes do not harden sufficiently when exposed, and even those which are known to be highly sensitive do not harden sufficiently.
  • An object of the present invention is to remedy the aforementioned drawbacks by providing a photosensitive recording material in which microcapsules can be sufficiently hardened with low energy, and which is capable of forming clear images with good tone and no smearing.
  • the present invention provides a photosensitive recording material comprising a support and microcapsules provided thereon, wherein the microcapsules comprises a photopolymerizable unsaturated group-containing compound and a phosphine compound represented by the following general formula: where R 1 , R 2 and R 3 indicate a hydrogen atom, a C 1 to C 20 alkyl, aryl or aralkyl group, -OR 4 , or -SR 4 where R 4 indicates a hydrogen atom or a C 1 to C 20 alkyl, aryl or aralkyl group, and these may be substituted by a halogen atom or a C 1 to C 20 alkoxy, alkoxycarbonyl, acyloxy, alkanoyl, cyano, hydroxy or amino group.
  • the microcapsules comprise the photopolymerizable unsaturated group-containing compound and the phosphine compound represented by the aforementioned general formula
  • the microcapsules are allowed to be sufficiently hardened with low energy, and clear images are also allowed to be formed with good tone and no smearing.
  • the photopolymerizable unsaturated group-containing compound is preferably a polymerizable compound having at least one ethylenic unsaturated double bond. This allows the microcapsules to be sufficiently cured rapidly, and clear images with good tone and no smearing to be formed.
  • the phosphine compound is contained in an amount of from 0.01 to 20 wt%. This allows the microcapsules to be sufficiently cured rapidly with low energy, and clear images with good tone and no smearing to be formed.
  • the photosensitive recording material of the present invention comprises a support and microcapsules provided thereon, where the microcapsules comprises a photopolymerizable unsaturated group-containing compound and a phosphine compound.
  • Examples of the aforementioned photopolymerizable unsaturated group-containing compound include compounds having ethylenic unsaturated groups and compounds having epoxy groups.
  • the compounds having ethylenic unsaturated groups with a relatively fast velocity of photopolymerization are especially preferred.
  • Examples of the compounds having ethylenic unsaturated groups include acrylic acid and salts thereof, acrylic acid esters, acrylamide, methacrylic acid and salts thereof, methacrylic acid esters, methacrylamides, maleic anhydride, maleic anhydride esters, itaconic acid esters, styrenes, vinyl ethers, vinyl esters, N -vinyl heterocycles, allyl ethers, allyl esters, and derivatives thereof.
  • acrylic acid esters or methacrylic acid esters with a relatively rapid degree of photopolymerization are especially preferred.
  • acrylic acid esters include butyl acrylate, cyclohexyl acrylate, ethylhexyl acrylate, benzyl acrylate, furfuryl acrylate, ethoxyethyl acrylate, tricyclodecanyloxy acrylate, nonylphenyloxyethyl arylate, hexanediol acrylate, 1,3-dioxolan acrylate, hexanediol diacrylate, butanediol diacrylate, neopentyl glycol diacrylate, polyethylene glycol diacrylate, tricyclodecane dimethylol diacrylate, tripropylene glycol diacrylate, bisphenol A diacrylate, pentaerythritol triacrylate, dipentaerythritol hexacrylate, dipentaerythritol caprolactone-adduct hexacrylate, trimethylol propane triacrylate, tri
  • methacrylic acid esters examples include butyl methacrylate, cyclohexyl methacrylate, ethylhexyl methacrylate, benzyl methacrylate, furfuryl methacrylate, ethoxyethyl methacrylate, tricyclodecanyloxy methacrylate, nonylphenyloxyethyl methacrylate, hexanediol methacrylate, 1,3-dioxolan methacrylate, hexanediol dimethacrylate, butanediol dimethacrylate, neopentyl glycol dimethacrylate, polyethylene glycol dimethacrylate, tricyclodecane dimethylol dimethacrylate, tripropylene glycol dimethacrylate, bisphenol A dimethacrylate, pentaerythritol trimethacrylate, dipentaerythritol hexamethacrylate,
  • These polymerizable compounds may be used individually or in combinations of two or more.
  • the aforementioned acrylic acid esters or methacrylic acid esters preferably contains at least one of pentaerythritol triacrylate, dipentaerythritol hexacrylate, dipentaerythritol caprolactone-adduct hexacrylate, trimethylol propane triacrylate, and trimethylol propane propylene oxide-adduct triacrylate, which have three or more aryloyl groups, which are unsaturated groups, per molecule.
  • the photopolymerizable unsaturated group-containing compound also contains the phosphine compound represented by the following general formula: where R 1 , R 2 and R 3 indicate a hydrogen atom, a C 1 to C 20 alkyl, aryl or aralkyl group, -OR 4 , or -SR 4 where R 4 indicates a hydrogen atom or a C 1 to C 20 alkyl, aryl or aralkyl group, and these may be substituted by a halogen atom or a C 1 to C 20 alkoxy, alkoxycarbonyl, acyloxy, alkanoyl, cyano, hydroxy or amino group.
  • R 1 , R 2 and R 3 indicate a hydrogen atom, a C 1 to C 20 alkyl, aryl or aralkyl group, -OR 4 , or -SR 4 where R 4 indicates a hydrogen atom or a C 1 to C 20 alkyl, aryl or aralkyl group, and these may be substitute
  • phosphine compounds include phosphate esters, phosphite esters, thiophosphate esters, thiophosphite esters, and derivatives thereof. Of these, thiophosphite derivatives with high sensitivity to light and good hardening properties are especially preferred.
  • the phosphine compound is added in an amount of 0.01 to 20 wt%, and preferably 0.5 to 10 wt%, with respect to the photopolymerizable unsaturated group-containing compound. Less than 0.01 wt% results in poor improvement, while more than 20 wt% results in extremely poor storage stability.
  • the photosensitive recording material of the present invention may contain a photopolymerization initiator, a photosensitizer such as a sensitizing colorant, a stabilizer such as a heat polymerization inhibitor, compatibility improving agent, a pigment or the like in addition to the aforementioned essential components.
  • a photopolymerization initiator such as a sensitizing colorant
  • a stabilizer such as a heat polymerization inhibitor
  • compatibility improving agent such as a pigment or the like in addition to the aforementioned essential components.
  • a highly sensitive photosensitive material can be obtained when a photopolymerization initiator or photosensitizer is added.
  • aromatic carbonyl compounds aromatic carbonyl compounds, acetophenones, organic peroxides, diphenylhalonium salts, organic halides, 2,4,6-substituted-S-triazines, 2,4,5-triarylimidazole dimers, azo compounds, dye borate complexes, metal arene complexes, titanocene compounds and the like can be used, which initiates or promotes the polymerization reaction of the aforementioned polymerizable material through light energy.
  • photopolymerization initiator benzophenone, benzyl, xanthone, thioxanthone, anthraquinone, acetophenone, 2,2-dimethl-2-morpholino-4'-methylthioacetophenone, benzoyl peroxide, 3,3',4,4'-tetrakis(t-butyldioxycarbonyl)benzophenone, diphenyl iodonium bromide, diphenyl iodonium chloride, carbon tetrachloride, carbon tetrabromide, 2,4,6-tristrichloromethyl-S-triazine, ( ⁇ 5 -2,4-cyclopentadien-1-yl)[(1,2,3,4,5,6- ⁇ )-(1-ethylethyl)benzene]iron(1+)hexafluorophosphate(1-), and the like are preferred. These photopolymerization initiator may be used individually or in combinations
  • the photopolymerization initiator is used in a ratio of 0.1 to 20 wt%, and preferably 1 to 10 wt%, with respect to the polymerizable material. Less than 1% ordinarily makes it difficult to produce a photopolymerization reaction, while more than 10% does not increase the sensitivity.
  • a sensitizing colorant may also be used to improve the photosensitivity, particularly the photosensitivity to wavelength, of the aforementioned photosensitive recording material.
  • Xanthene dyes As the sensitizing colorant, Xanthene dyes, coumarin dyes, mellocyanine dyes, thiazine dyes, azine dyes, methine dyes, oxazine dyes, phenylmethane dyes, cyanine dyes, azo dyes, anthraquinone dyes, pyrazoline dyes, stilbene dyes, quinoline dyes, and the like can be used.
  • Pigments can be used as a coloring material. Those of suitable hue may be selected from those that are commercially available as well as those listed in Pigments manuals or other such documents (such as New Pigment Manual [Saishin Ganryo Benran], compiled by Nihon Ganryo Gijutsu Kyokai and published in 1977) in the literature, and are dispersed for use.
  • Organic solvents having suitable polarity can also be used to adjust the solubility of the composition encapsulated in the microcapsules of the present invention.
  • microcapsules can be manufactured using encapsulation methods which are already well known techniques in the field.
  • the methods include phase separation methods from aqueous solutions such as those disclosed in U.S. Patents No. 2,800,457 and 2,800,458, interfacial polymerization methods such as that disclosed in Japanese Patent Publications No. 38-19574, 42-446, and 42-771, in-situ methods based on the polymerization of monomers such as those disclosed in Japanese Patent Publication No. 36-9168 and Japanese Patent Application Laid-Open No. 51-9079, and catalytic dispersion cooling method such as that disclosed in Great Britain Patents No. 952,807 and 965,074.
  • microcapsule wall-forming material any inorganic or organic materials, as long as microcapsule walls can be made therefrom in the aforementioned capsule manufacturing methods, can be used.
  • the microcapsule wall-forming material is preferably to exhibit excellent light-transmissive.
  • microcapsule wall-forming material examples include gelatin, gum arabic, starch, sodium alginate, polyvinyl alcohol, polyethylene, polyamides, polyester, polyurethane, polyurea, polystyrene, nitrocellulose, ethylcellulose, methylcellulose, melamine-formaldehyde resins, urea-formaldehyde resins, and the like, as well as copolymers thereof.
  • Melamine-formaldehyde resins or urea-formaldehyde resins which can be produced in a relatively simple manufacturing method, are preferred when the in-situ method is used, in which the wall starting material is supplied in water.
  • the composition serving as the encapsulation material must be dispersed or emulsified in an aqueous medium.
  • the aqueous medium should contain a nonionic or anionic water-soluble polymer.
  • nonionic water-soluble polymers examples include polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylamide, polymethylvinyl ether, hydroxymethylcellulose, and hydroxyethylcellulose.
  • anionic water-soluble polymers examples include polystyrenesulfinic acid, polystyrenesulfonates, styrenesulfonic acid copolymers, polyvinyl sulfuric acid ester salts, polyvinylsulfonates, maleic anhydride-styrene copolymers, and maleic anhydride-isobutylene copolymers.
  • Examples of materials used as the recording medium for the photosensitive recording material of the present invention include paper, high grade paper, coated paper and other types of paper; films and resins such as polyester, polyethylene, polypropylene, cellulose acetate, cellulose ester, polyvinyl acetal, polystyrene, polycarbonate, polyethylene terephthalate, or polyimide; and synthetic paper or the like comprising paper and resin.
  • films are preferred because they have excellent surface smoothness, strength, and the like, and because they are thin, with a thickness of not more than 0.05 mm and they therefore have a relatively small volume area when rolled. Forming a reflection layer by aluminum deposition or the like on at least one side of the film is effective for improving the photosensitivity of the photosensitive recording material.
  • a hydrophilic binder is mixed in the microcapsule dispersed liquid to form a photosensitive layer by applying the microcapsules on the aforementioned recording medium.
  • Natural substances such as gelatin, cellulose, starch, and gum arabic, or synthetic polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylic acid, polymethacrylic acid, polyacrylamide, polyvinyl imidazole, and polystyrenesulfonic acid may be used as the hydrophilic binder.
  • a photosensitive recording material using microcapsules containing a phosphine compound with the following composition and a photosensitive recording material using microcapsules containing no phosphine compound were applied to the surface of polyester sheets.
  • the materials were exposed and hardened using a spectral sensitivity meter, and were then overlaid with image-receiving paper and pressurized.
  • the hardening energy was measured based on the extent of hardness at the maximum image hardness wavelength, the radiating energy from the light source at that wavelength, and the exposure time, and the obtained value was considered an index of hardness.
  • R 1 , R 2 , and R 3 are all -SR 4 , and R 4 is a C 12 straight-chain alkyl group.
  • R 1 , R 2 , and R 3 are all C 6 aryl groups.
  • R 1 , R 2 , and R 3 are all -OR 4 , and R 4 is a C 6 aryl group.
  • the photosensitive recording materials in which the photopolymerizable unsaturated group-containing compound contained a phosphine compound can thus be said to be more sensitive to light and to have good hardening properties.
  • the photosensitive recording material of the present invention allows the microcapsules to be sufficiently hardened with low energy, and clear images to be formed with good tone and no smearing.
  • the photosensitive recording material of the present invention in which the photopolymerizable unsaturated group-containing compound is a polymerizable compound containing at least one ethylenic unsaturated double bond, allows the microcapsules to be sufficiently hardened rapidly, and clear images to be formed with good tone and no smearing.
  • the photosensitive recording material of the present invention in which the phosphine compound is present in an amount of from about 0.01 to 20 wt%, allows the microcapsules to be sufficiently hardened in a rapid manner with low energy, and clear images to be formed with good tone and no smearing.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Materials For Photolithography (AREA)
  • Photosensitive Polymer And Photoresist Processing (AREA)
  • Manufacturing Of Micro-Capsules (AREA)

Abstract

A photosensitive recording material comprising a support and microcapsules provided thereon, wherein the microcapsules comprise a photopolymerizable unsaturated group-containing compound and a phosphine compound represented by the following general formula:
Figure 80000001
in which R1, R2 and R3 each independently represent a hydrogen atom, a C1 to C20 alkyl, aryl or aralkyl group, -OR4, or -SR4 where R4 represents a hydrogen atom or a C1 to C20 alkyl, aryl or aralkyl group, these groups being optionally substituted by one or more of the same or different substituents selected from halogen atoms and C1 to C20 alkoxy, alkoxycarbonyl, acyloxy, alkanoyl, cyano, hydroxy and amino groups.

Description

BACKBROPUND OF THE INVENTION 1. Field of the Invention
The present invention relates to a photosensitive recording material using microcapsules, and in particular to a photosensitive recording material using microcapsules that contain core materials in a specific combination.
2. Related Art of the Invention
Conventional photosensitive recording materials, such as that disclosed in Japanese Patent Application Laid-Open No. 57-124343, have been used as recording materials in which microcapsules are supported on a recording medium such as paper or the like.
In such photosensitive recording materials, the microcapsules are commonly applied over the entire surface of the recording medium, the surface of the photosensitive recording material is exposed to form a latent image based on the image that is to be recorded, and the recording medium on which the latent image has been formed is pressurized to visualize and record the image.
That is, the microcapsules harden in the portions that is exposed, but do not harden in the unexposed portions, and since the capsules themselves are not destroyed by pressure in the portions where the microcapsules have hardened, they do not colorize in the portions where they have hardened when the recording medium on which the latent image has been formed is pressurized by a pressurization device, while the microcapsules are destroyed according to the wavelength of the exposure light in the portions where the capsules have not hardened, resulting in the development of color by a coloring reaction.
However, a problem in conventional photosensitive recording materials using microcapsules is that the microcapsules sometimes do not harden sufficiently when exposed, and even those which are known to be highly sensitive do not harden sufficiently.
Although there are methods for increasing the radiation energy of the exposure or the exposure time to ensure that the aforementioned photosensitive recording material is sufficiently hardened, a problem is the resulting increase in the size and cost of the exposure equipment.
SUMMARY OF THE INVENTION
An object of the present invention is to remedy the aforementioned drawbacks by providing a photosensitive recording material in which microcapsules can be sufficiently hardened with low energy, and which is capable of forming clear images with good tone and no smearing.
To achieve this object, the present invention provides a photosensitive recording material comprising a support and microcapsules provided thereon, wherein the microcapsules comprises a photopolymerizable unsaturated group-containing compound and a phosphine compound represented by the following general formula:
Figure 00030001
where R1, R2 and R3 indicate a hydrogen atom, a C1 to C20 alkyl, aryl or aralkyl group, -OR4, or -SR4 where R4 indicates a hydrogen atom or a C1 to C20 alkyl, aryl or aralkyl group, and these may be substituted by a halogen atom or a C1 to C20 alkoxy, alkoxycarbonyl, acyloxy, alkanoyl, cyano, hydroxy or amino group.
According to the photosensitive recording material of the present invention in which the microcapsules comprise the photopolymerizable unsaturated group-containing compound and the phosphine compound represented by the aforementioned general formula, the microcapsules are allowed to be sufficiently hardened with low energy, and clear images are also allowed to be formed with good tone and no smearing.
In the photosensitive recording material of the present invention, the photopolymerizable unsaturated group-containing compound is preferably a polymerizable compound having at least one ethylenic unsaturated double bond. This allows the microcapsules to be sufficiently cured rapidly, and clear images with good tone and no smearing to be formed.
In the photosensitive recording material of the present invention, it is preferably that the phosphine compound is contained in an amount of from 0.01 to 20 wt%. This allows the microcapsules to be sufficiently cured rapidly with low energy, and clear images with good tone and no smearing to be formed.
This and other objects, features and advantages of the present invention are described in or will become apparent from the following detailed description of the invention.
DETAILED DESCRIPTION OF THE INVENTION
The photosensitive recording material of the present invention comprises a support and microcapsules provided thereon, where the microcapsules comprises a photopolymerizable unsaturated group-containing compound and a phosphine compound.
Examples of the aforementioned photopolymerizable unsaturated group-containing compound include compounds having ethylenic unsaturated groups and compounds having epoxy groups. The compounds having ethylenic unsaturated groups with a relatively fast velocity of photopolymerization are especially preferred.
Examples of the compounds having ethylenic unsaturated groups include acrylic acid and salts thereof, acrylic acid esters, acrylamide, methacrylic acid and salts thereof, methacrylic acid esters, methacrylamides, maleic anhydride, maleic anhydride esters, itaconic acid esters, styrenes, vinyl ethers, vinyl esters, N-vinyl heterocycles, allyl ethers, allyl esters, and derivatives thereof. Of these, acrylic acid esters or methacrylic acid esters with a relatively rapid degree of photopolymerization are especially preferred.
Specific examples of acrylic acid esters include butyl acrylate, cyclohexyl acrylate, ethylhexyl acrylate, benzyl acrylate, furfuryl acrylate, ethoxyethyl acrylate, tricyclodecanyloxy acrylate, nonylphenyloxyethyl arylate, hexanediol acrylate, 1,3-dioxolan acrylate, hexanediol diacrylate, butanediol diacrylate, neopentyl glycol diacrylate, polyethylene glycol diacrylate, tricyclodecane dimethylol diacrylate, tripropylene glycol diacrylate, bisphenol A diacrylate, pentaerythritol triacrylate, dipentaerythritol hexacrylate, dipentaerythritol caprolactone-adduct hexacrylate, trimethylol propane triacrylate, trimethylol propane propylene oxide-adduct triacrylate, polyoxyethylenated bisphenol A diacrylate, polyester acrylate, and polyurethane acrylate.
Examples of methacrylic acid esters include butyl methacrylate, cyclohexyl methacrylate, ethylhexyl methacrylate, benzyl methacrylate, furfuryl methacrylate, ethoxyethyl methacrylate, tricyclodecanyloxy methacrylate, nonylphenyloxyethyl methacrylate, hexanediol methacrylate, 1,3-dioxolan methacrylate, hexanediol dimethacrylate, butanediol dimethacrylate, neopentyl glycol dimethacrylate, polyethylene glycol dimethacrylate, tricyclodecane dimethylol dimethacrylate, tripropylene glycol dimethacrylate, bisphenol A dimethacrylate, pentaerythritol trimethacrylate, dipentaerythritol hexamethacrylate, dipentaerythritol caprolactone-adduct hexamethacrylate, trimethylol propane trimethacrylate, trimethylol propane propylene oxide-adduct trimethacrylate, polyoxyethylenated bisphenol A dimethacrylate, polyester methacrylate, and polyurethane methacrylate.
These polymerizable compounds may be used individually or in combinations of two or more.
The aforementioned acrylic acid esters or methacrylic acid esters preferably contains at least one of pentaerythritol triacrylate, dipentaerythritol hexacrylate, dipentaerythritol caprolactone-adduct hexacrylate, trimethylol propane triacrylate, and trimethylol propane propylene oxide-adduct triacrylate, which have three or more aryloyl groups, which are unsaturated groups, per molecule.
The photopolymerizable unsaturated group-containing compound also contains the phosphine compound represented by the following general formula:
Figure 00070001
where R1, R2 and R3 indicate a hydrogen atom, a C1 to C20 alkyl, aryl or aralkyl group, -OR4, or -SR4 where R4 indicates a hydrogen atom or a C1 to C20 alkyl, aryl or aralkyl group, and these may be substituted by a halogen atom or a C1 to C20 alkoxy, alkoxycarbonyl, acyloxy, alkanoyl, cyano, hydroxy or amino group.
Examples of phosphine compounds include phosphate esters, phosphite esters, thiophosphate esters, thiophosphite esters, and derivatives thereof. Of these, thiophosphite derivatives with high sensitivity to light and good hardening properties are especially preferred.
The phosphine compound is added in an amount of 0.01 to 20 wt%, and preferably 0.5 to 10 wt%, with respect to the photopolymerizable unsaturated group-containing compound. Less than 0.01 wt% results in poor improvement, while more than 20 wt% results in extremely poor storage stability.
The photosensitive recording material of the present invention may contain a photopolymerization initiator, a photosensitizer such as a sensitizing colorant, a stabilizer such as a heat polymerization inhibitor, compatibility improving agent, a pigment or the like in addition to the aforementioned essential components. A highly sensitive photosensitive material can be obtained when a photopolymerization initiator or photosensitizer is added.
As the photopolymerization initiator, aromatic carbonyl compounds, acetophenones, organic peroxides, diphenylhalonium salts, organic halides, 2,4,6-substituted-S-triazines, 2,4,5-triarylimidazole dimers, azo compounds, dye borate complexes, metal arene complexes, titanocene compounds and the like can be used, which initiates or promotes the polymerization reaction of the aforementioned polymerizable material through light energy.
Specifically as the photopolymerization initiator, benzophenone, benzyl, xanthone, thioxanthone, anthraquinone, acetophenone, 2,2-dimethl-2-morpholino-4'-methylthioacetophenone, benzoyl peroxide, 3,3',4,4'-tetrakis(t-butyldioxycarbonyl)benzophenone, diphenyl iodonium bromide, diphenyl iodonium chloride, carbon tetrachloride, carbon tetrabromide, 2,4,6-tristrichloromethyl-S-triazine, (η5-2,4-cyclopentadien-1-yl)[(1,2,3,4,5,6-η)-(1-ethylethyl)benzene]iron(1+)hexafluorophosphate(1-), and the like are preferred. These photopolymerization initiator may be used individually or in combinations of two or more.
The photopolymerization initiator is used in a ratio of 0.1 to 20 wt%, and preferably 1 to 10 wt%, with respect to the polymerizable material. Less than 1% ordinarily makes it difficult to produce a photopolymerization reaction, while more than 10% does not increase the sensitivity.
A sensitizing colorant may also be used to improve the photosensitivity, particularly the photosensitivity to wavelength, of the aforementioned photosensitive recording material.
As the sensitizing colorant, Xanthene dyes, coumarin dyes, mellocyanine dyes, thiazine dyes, azine dyes, methine dyes, oxazine dyes, phenylmethane dyes, cyanine dyes, azo dyes, anthraquinone dyes, pyrazoline dyes, stilbene dyes, quinoline dyes, and the like can be used.
Pigments can be used as a coloring material. Those of suitable hue may be selected from those that are commercially available as well as those listed in Pigments manuals or other such documents (such as New Pigment Manual [Saishin Ganryo Benran], compiled by Nihon Ganryo Gijutsu Kyokai and published in 1977) in the literature, and are dispersed for use.
The use of monoazos, disazos, azocalcium Lake, and azobarium Lake for yellow, of quinacridone and calcium Lake for magenta, and of phthalocyanine and the like for cyan, is particularly preferred.
Organic solvents having suitable polarity can also be used to adjust the solubility of the composition encapsulated in the microcapsules of the present invention.
Such microcapsules can be manufactured using encapsulation methods which are already well known techniques in the field. Examples of the methods include phase separation methods from aqueous solutions such as those disclosed in U.S. Patents No. 2,800,457 and 2,800,458, interfacial polymerization methods such as that disclosed in Japanese Patent Publications No. 38-19574, 42-446, and 42-771, in-situ methods based on the polymerization of monomers such as those disclosed in Japanese Patent Publication No. 36-9168 and Japanese Patent Application Laid-Open No. 51-9079, and catalytic dispersion cooling method such as that disclosed in Great Britain Patents No. 952,807 and 965,074.
As the microcapsule wall-forming material, any inorganic or organic materials, as long as microcapsule walls can be made therefrom in the aforementioned capsule manufacturing methods, can be used. The microcapsule wall-forming material is preferably to exhibit excellent light-transmissive.
Specific examples of the microcapsule wall-forming material include gelatin, gum arabic, starch, sodium alginate, polyvinyl alcohol, polyethylene, polyamides, polyester, polyurethane, polyurea, polystyrene, nitrocellulose, ethylcellulose, methylcellulose, melamine-formaldehyde resins, urea-formaldehyde resins, and the like, as well as copolymers thereof.
Melamine-formaldehyde resins or urea-formaldehyde resins, which can be produced in a relatively simple manufacturing method, are preferred when the in-situ method is used, in which the wall starting material is supplied in water.
When the microcapsules are thus manufactured, the composition serving as the encapsulation material must be dispersed or emulsified in an aqueous medium. At this time, the aqueous medium should contain a nonionic or anionic water-soluble polymer.
Examples of nonionic water-soluble polymers include polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylamide, polymethylvinyl ether, hydroxymethylcellulose, and hydroxyethylcellulose.
Examples of anionic water-soluble polymers include polystyrenesulfinic acid, polystyrenesulfonates, styrenesulfonic acid copolymers, polyvinyl sulfuric acid ester salts, polyvinylsulfonates, maleic anhydride-styrene copolymers, and maleic anhydride-isobutylene copolymers.
Examples of materials used as the recording medium for the photosensitive recording material of the present invention include paper, high grade paper, coated paper and other types of paper; films and resins such as polyester, polyethylene, polypropylene, cellulose acetate, cellulose ester, polyvinyl acetal, polystyrene, polycarbonate, polyethylene terephthalate, or polyimide; and synthetic paper or the like comprising paper and resin. Of these, films are preferred because they have excellent surface smoothness, strength, and the like, and because they are thin, with a thickness of not more than 0.05 mm and they therefore have a relatively small volume area when rolled. Forming a reflection layer by aluminum deposition or the like on at least one side of the film is effective for improving the photosensitivity of the photosensitive recording material.
A hydrophilic binder is mixed in the microcapsule dispersed liquid to form a photosensitive layer by applying the microcapsules on the aforementioned recording medium. Natural substances such as gelatin, cellulose, starch, and gum arabic, or synthetic polymers such as polyvinyl alcohol, polyvinyl pyrrolidone, polyacrylic acid, polymethacrylic acid, polyacrylamide, polyvinyl imidazole, and polystyrenesulfonic acid may be used as the hydrophilic binder.
EXAMPLES
The present invention will be illustrated in further detail below through the following working examples. The present invention should not be limited to the examples.
Examples 1 to 3 and Comparative Example 1
A photosensitive recording material using microcapsules containing a phosphine compound with the following composition and a photosensitive recording material using microcapsules containing no phosphine compound were applied to the surface of polyester sheets.
The materials were exposed and hardened using a spectral sensitivity meter, and were then overlaid with image-receiving paper and pressurized.
The hardening energy was measured based on the extent of hardness at the maximum image hardness wavelength, the radiating energy from the light source at that wavelength, and the exposure time, and the obtained value was considered an index of hardness.
Encapsulation Material for Microcapsule
  • (a) photopolymerizable unsaturated group-containing compound (1:1 blend)    100 parts by weight
    dipentaerythritol polyacrylate
    phenyl glycidyl ether acrylate
  • (b) photopolymerization initiator iron arene complex   4 parts by weight
  • (c) wavelength sensitizing dye squarilium dyes   0.3 parts by weight
  • (d) sensitizing dye 2,6-diisopropyl-N,N-dimethylaniline   1.5 parts by weight
  • (e) phosphine compound    4 parts by weight
    • The results are given in Table 1.
    (Exposure light-wavelength:650nm)
    Composition No. Phosphine compound Hardening energy (erg·cm-2)
    Example 1 trilauryl thiophosphite 2,000
    Example 2 triphenylphosphine 5,200
    Example 3 triphenylphosphite 3,300
    Comparative Example 1 none added 10,000
    The phosphine compounds used in the examples 1 to 3 shown in Table 1 above are given below.
    In the phosphine compound of the aforementioned general formula in Example 1, R1, R2, and R3 are all -SR4, and R4 is a C12 straight-chain alkyl group. In the phosphine compound in Example 2, R1, R2, and R3 are all C6 aryl groups.
    In the phosphine compound in Example 3, R1, R2, and R3 are all -OR4, and R4 is a C6 aryl group.
    The results in Table 1 show that Examples 1 to 3, in which a phosphine compound was used, had lower exposure energy levels and faster hardening velocities than Comparative Example 1, in which no phosphine compound was contained.
    The photosensitive recording materials in which the photopolymerizable unsaturated group-containing compound contained a phosphine compound can thus be said to be more sensitive to light and to have good hardening properties.
    As is clear in the description above, the photosensitive recording material of the present invention allows the microcapsules to be sufficiently hardened with low energy, and clear images to be formed with good tone and no smearing.
    The photosensitive recording material of the present invention, in which the photopolymerizable unsaturated group-containing compound is a polymerizable compound containing at least one ethylenic unsaturated double bond, allows the microcapsules to be sufficiently hardened rapidly, and clear images to be formed with good tone and no smearing.
    The photosensitive recording material of the present invention, in which the phosphine compound is present in an amount of from about 0.01 to 20 wt%, allows the microcapsules to be sufficiently hardened in a rapid manner with low energy, and clear images to be formed with good tone and no smearing.
    The entire disclosure of the specification, claims and summary of Japanese Patent Application No. 9-130813 filed on May 21, 1997 is herein incorporated by reference in its entirety.

    Claims (18)

    1. A photosensitive recording material comprising a support and microcapsules provided thereon, wherein the microcapsules comprise a photopolymerizable unsaturated group-containing compound and a phosphine compound represented by the following general formula:
      Figure 00170001
      in which R1, R2 and R3 each independently represent a hydrogen atom, a C1 to C20 alkyl, aryl or aralkyl group, -OR4, or -SR4 where R4 represents a hydrogen atom or a C1 to C20 alkyl, aryl or aralkyl group, these groups being optionally substituted by one or more of the same or different substituents selected from halogen atoms and C1 to C20 alkoxy, alkoxycarbonyl, acyloxy, alkanoyl, cyano, hydroxy and amino groups.
    2. A recording material according to claim 1, wherein said photopolymerizable unsaturated group-containing compound is a polymerizable compound having at least one ethylenic unsaturated double bond.
    3. A recording material according to claim 2, wherein the polymerizable compound is selected from acrylic acid and salts thereof, acrylic acid esters, acrylamide, methacrylic acid and salts thereof, methacrylic acid esters, methacrylamides, maleic anhydride, maleic anhydride esters, itaconic acid esters, styrenes, vinyl ethers, vinyl esters, N-vinyl heterocycles, allyl ethers, allyl esters, and derivatives thereof.
    4. A recording material according to claim 3, wherein the polymerizable compound is selected from acrylic acid esters and methacrylic acid esters.
    5. A recording material according to claim 4, wherein the acrylic acid ester is selected from butyl acrylate, cyclohexyl acrylate, ethylhexyl acrylate, benzyl acrylate, furfuryl acrylate, ethoxyethyl acrylate, tricyclodecanyloxy acrylate, nonylphenyloxyethyl acrylate, hexanediol acrylate, 1,3-dioxolan acrylate, hexanediol diacrylate, butenediol diacrylate, neopentyl glycol diacrylate, polyethylene glycol diacrylate, tricyclodecane dimethylol diacrylate, tripropylene glycol diacrylate, bisphenol A diacrylate, pentaerythritol triacrylate, dipentaerythritol triacrylate, dipentaerythritol hexacrylate, dipentaerythritol caprolactone-adduct hexacrylate, trimethylol propane triacrylate, trimethylol propane propylene oxide-adduct triacrylate, polyoxyethylenated bisphenol A diacrylate, polyester acrylate, and polyurethane acrylate.
    6. A recording material according to claim 4, wherein the methacrylic acid ester is selected butyl methacrylate, cyclohexyl methacrylate, ethylhexyl methacrylate, benzyl methacrylate, furfuryl methacrylate, ethoxyethyl methacrylate, tricyclodecanyloxy methacrylate, nonylphenyloxyethyl methacrylate, hexanediol methacrylate, 1,3-dioxolan methacrylate, hexanediol dimethylacrylate, butanediol dimethylacrylate, neopentyl glycol dimethacrylate, polyethylene glycol dimethacrylate, tricyclodecane dimethylol dimethacrylate, tripropylene glycol dimethacrylate, bisphenol A dimethacrylate, pentaerythritol trimethacrylate, dipentaerythritol hexamethacrylate, dipentaerythritol caprolactone-adduct hexamethacrylate, trimethylol propane trimethacrylate, trimethylol propane propylene oxide-adduct trimethacrylate, polyoxyethylenated bisphenol A dimethacrylate, polyester methacrylate, and polyurethane methacrylate.
    7. A recording material according to claim 4, wherein the polymerizable compound contains at least one of pentaerythritol triacrylate, dipentaerythritol hexacrylate, dipentaerythritol caprolactone-adduct hexacrylate, trimethylol propane triacrylate, and trimethylol propane propylene oxide-adduct triacrylate.
    8. A recording material according to any one of the preceding claims, wherein said phosphine compound is present in an amount of from about 0.01 to 20 wt% based on the weight of the photopolymerizable unsaturated-group containing compound.
    9. A recording material according to claim 8, wherein said phosphine compound is present in an amount of from about 0.5 to 10 wt% based on the weight of the photopolymerizable unsaturated-group containing compound.
    10. A recording material according to any one of the preceding claims, wherein said phosphine compound is selected front phosphate esters, phosphite esters, thiophosphate esters, thiophosphite esters, and derivatives thereof.
    11. A recording material according to claim 10, wherein said phosphine compound includes at least one thiophosphite derivative.
    12. A recording material according to any one of the preceding claims, wherein the microcapsules contain a photopolymerisation initiator.
    13. A recording material according to claim 12, wherein the photopolymerisation initiator is selected from aromatic carbonyl compounds, acetophenones, organic peroxides, diphenylhalonium salts, organic halides, 2,4,6-substituted-S-triazines, 2,4,5-triarylimidazole dimers, azo compounds, dye borate complexes, metal arene complexes, and titanocene compounds.
    14. A recording material according to claim 13, wherein the photopolymerisation initiator is selected from benzophenone, benzyl, xanthone, thioxanthone, anthraquinone, acetophenone, 2, 2-dimethyl -2-morpholino-4'-methylthioacetophenone, benzoyl peroxide, 3,3', 4,4'-tetrakis(t-butyldioxycarbonyl)benzophenone, diphenyl iodonium bromide, diphenyl iodonium chloride, carbon tetrachloride, carbon tetrabromide, 2, 4, 6-tristrichloromethyl-S-triazine, and (η5-2,4-cyclopentadienl-yl) [1,2,3,4,5,6-η) - (1-ethylethyl)benzene] iron (1+) hexafluorophosphate (1-).
    15. A recording material according to any one of claims 12 to 14, wherein the microcapsules contain from 0.1 to 20 wt% of photopolymerization initiator.
    16. A recording material according to claim 15, wherein the microcapsules contain from 1 to 10 wt% of photopolymerization initiator.
    17. A recording material according to any one of the preceding claims, wherein the microcapsules contain a sensitizing colorant as a photosensitizer.
    18. A recording material according to claim 17, wherein the sensitizing colorant is selected from Xanthene dyes, coumarin dyes, mellocyanine dyes, thiazine dyes, azine dyes, methine dyes, oxazine dyes, phenylmethane dyes, cyanine dyes, azo dyes, anthraquinone dyes, pyrazoline dyes, stilbene dyes, and quinoline dyes.
    EP98304014A 1997-05-21 1998-05-20 Photosensitive recording material using microcapsules Withdrawn EP0884650A1 (en)

    Applications Claiming Priority (2)

    Application Number Priority Date Filing Date Title
    JP130813/97 1997-05-21
    JP9130813A JPH10319584A (en) 1997-05-21 1997-05-21 Photosensitive recording material using microcapsules

    Publications (1)

    Publication Number Publication Date
    EP0884650A1 true EP0884650A1 (en) 1998-12-16

    Family

    ID=15043319

    Family Applications (1)

    Application Number Title Priority Date Filing Date
    EP98304014A Withdrawn EP0884650A1 (en) 1997-05-21 1998-05-20 Photosensitive recording material using microcapsules

    Country Status (3)

    Country Link
    US (1) US6117609A (en)
    EP (1) EP0884650A1 (en)
    JP (1) JPH10319584A (en)

    Cited By (2)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    WO2000029453A1 (en) * 1998-11-18 2000-05-25 Taiyo Ink Manufacturing Co., Ltd. Photocurable composition
    WO2006063891A1 (en) * 2004-12-15 2006-06-22 Degussa Ag Radically homo- or copolymerizable compounds, method for the production and use thereof

    Families Citing this family (6)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    BRPI0313763B8 (en) * 2002-08-19 2021-05-25 4325231 Canada Inc 2,4,5-trisubstituted imidazoles, their uses, and pharmaceutical and antimicrobial compositions
    DK1692113T3 (en) * 2003-11-14 2018-01-08 Lorus Therapeutics Inc ARYLIMIDAZOLES AND USE THEREOF AS ANTICANCES
    ES2473597T3 (en) * 2005-05-25 2014-07-07 Lorus Therapeutics Inc. Derivatives of 2-indolyl imidazo [4,5-d] phenanthroline and its use in cancer treatment
    EP2976342A4 (en) 2013-03-20 2016-08-10 Aptose Biosciences Inc 2-substituted imidazo[4,5-d]phenanthroline derivatives and their use in the treatment of cancer
    US9567643B2 (en) 2013-10-04 2017-02-14 Aptose Biosciences Inc. Compositions and methods for treating cancers
    CN111417395A (en) 2017-10-30 2020-07-14 艾普托斯生物科学公司 Arylimidazoles for the treatment of cancer

    Citations (11)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    US4116788A (en) * 1975-11-21 1978-09-26 Espe Fabrik Pharmazeutischer Praparate Gmbh Process for the photopolymerization of acrylic acid ester-containing compositions
    US4283481A (en) * 1978-09-11 1981-08-11 Napp Systems (Usa) Inc. Element having phosphine activated photosensitive compositions therein
    US4289844A (en) * 1979-06-18 1981-09-15 Eastman Kodak Company Photopolymerizable compositions featuring novel co-initiators
    US4522693A (en) * 1980-09-15 1985-06-11 Basf Aktiengesellschaft Photopolymerizable composition with acylphosphine sulfide photoinitiator and method
    EP0223587A1 (en) * 1985-11-20 1987-05-27 The Mead Corporation Photosensitive materials containing ionic dye compounds as initiators
    US4868091A (en) * 1986-10-01 1989-09-19 Basf Aktiengesellschaft Photopolymerizable recording material, in particular for the production of printing plates and relief plates
    US4940645A (en) * 1985-07-16 1990-07-10 The Mead Corporation Imaging material employing photosensitive microcapsules containing tertiary amines as coinitiators
    US5055372A (en) * 1990-04-23 1991-10-08 The Mead Corporation Photohardenable composition containing borate salts and ketone initiators
    US5124236A (en) * 1987-07-06 1992-06-23 Fuji Photo Film Co., Ltd. Photopolymerizable composition
    EP0523565A1 (en) * 1991-07-15 1993-01-20 Fuji Photo Film Co., Ltd. Light-sensitive material containing silver halide, reducing agent, polymerizable compound and color imager forming substance
    EP0560724A1 (en) * 1992-03-11 1993-09-15 Ciba-Geigy Ag Benzoyl substituted phosphabicycloalcanes and their sulphides as photoinitiators

    Family Cites Families (11)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    GB965074A (en) * 1900-01-01
    NL95044C (en) * 1953-06-30
    US2800457A (en) * 1953-06-30 1957-07-23 Ncr Co Oil-containing microscopic capsules and method of making them
    BE622026A (en) * 1961-09-05
    JPS3819574B1 (en) * 1961-11-16 1963-09-26
    JPS42446Y1 (en) * 1964-12-29 1967-01-12
    US4001140A (en) * 1974-07-10 1977-01-04 Ncr Corporation Capsule manufacture
    JPS57124343A (en) * 1981-01-26 1982-08-03 Fuji Photo Film Co Ltd Microcapsule and photosensitive material using it
    US4576891A (en) * 1984-06-15 1986-03-18 The Mead Corporation Photosensitive microcapsules useful in polychromatic imaging having radiation absorber
    JP2775880B2 (en) * 1989-08-21 1998-07-16 ブラザー工業株式会社 Transfer recording medium
    JPH08206489A (en) * 1995-02-09 1996-08-13 Brother Ind Ltd Photo-curing composition and photosensitive capsule

    Patent Citations (11)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    US4116788A (en) * 1975-11-21 1978-09-26 Espe Fabrik Pharmazeutischer Praparate Gmbh Process for the photopolymerization of acrylic acid ester-containing compositions
    US4283481A (en) * 1978-09-11 1981-08-11 Napp Systems (Usa) Inc. Element having phosphine activated photosensitive compositions therein
    US4289844A (en) * 1979-06-18 1981-09-15 Eastman Kodak Company Photopolymerizable compositions featuring novel co-initiators
    US4522693A (en) * 1980-09-15 1985-06-11 Basf Aktiengesellschaft Photopolymerizable composition with acylphosphine sulfide photoinitiator and method
    US4940645A (en) * 1985-07-16 1990-07-10 The Mead Corporation Imaging material employing photosensitive microcapsules containing tertiary amines as coinitiators
    EP0223587A1 (en) * 1985-11-20 1987-05-27 The Mead Corporation Photosensitive materials containing ionic dye compounds as initiators
    US4868091A (en) * 1986-10-01 1989-09-19 Basf Aktiengesellschaft Photopolymerizable recording material, in particular for the production of printing plates and relief plates
    US5124236A (en) * 1987-07-06 1992-06-23 Fuji Photo Film Co., Ltd. Photopolymerizable composition
    US5055372A (en) * 1990-04-23 1991-10-08 The Mead Corporation Photohardenable composition containing borate salts and ketone initiators
    EP0523565A1 (en) * 1991-07-15 1993-01-20 Fuji Photo Film Co., Ltd. Light-sensitive material containing silver halide, reducing agent, polymerizable compound and color imager forming substance
    EP0560724A1 (en) * 1992-03-11 1993-09-15 Ciba-Geigy Ag Benzoyl substituted phosphabicycloalcanes and their sulphides as photoinitiators

    Cited By (2)

    * Cited by examiner, † Cited by third party
    Publication number Priority date Publication date Assignee Title
    WO2000029453A1 (en) * 1998-11-18 2000-05-25 Taiyo Ink Manufacturing Co., Ltd. Photocurable composition
    WO2006063891A1 (en) * 2004-12-15 2006-06-22 Degussa Ag Radically homo- or copolymerizable compounds, method for the production and use thereof

    Also Published As

    Publication number Publication date
    US6117609A (en) 2000-09-12
    JPH10319584A (en) 1998-12-04

    Similar Documents

    Publication Publication Date Title
    CN1882879B (en) Photopolymerizable composition
    JP2834213B2 (en) Photopolymerizable mixtures, recording materials made therefrom, and methods of making copies
    US6242149B1 (en) Fast-curing photosensitive composition and recording sheet
    JPS62143044A (en) Photosetting composition containing dye borate complex and photosensitive material using the same
    JP3185585B2 (en) Photocurable composition and photosensitive capsule
    US6117609A (en) Photosensitive recording material using microcapsules
    EP0557555B1 (en) Photopolymerizable composition
    JP2897375B2 (en) Photopolymerizable composition
    GB2162652A (en) Photosensitive microcapsules and their use in imaging systems
    EP0379200A2 (en) Photopolymerizable composition
    US5686220A (en) Photo-curing composition and photosensitive capsule
    US5955237A (en) Photosensitive recording medium exposed by three exposure wavelengths longer than 500 nm
    JPH03138189A (en) Image receiving material
    US6342329B1 (en) Image-forming medium
    EP0422662B1 (en) Light-sensitive material containing silver halide, reducing agent, polymerizable compound, color image forming substance, base precursor and polar compound
    JPH08217810A (en) Photo-setting composition and photosensitive capsule
    JPH0990619A (en) Photosetting composition and photosensitive capsule
    JPH09258436A (en) Photosensitive microcapsule
    JP2897369B2 (en) Photopolymerizable composition
    US6846605B2 (en) Photopolymerizable composition and recording material using same
    JP2002244283A (en) Polymerizable composition and optical recording material
    JPH09265185A (en) Photosensitive microcapsule
    JPH11171909A (en) Photopolymerizable composition and sheet for recording
    JPH09269595A (en) Photosensitive microcapsule
    JPH1195422A (en) Photosensitive material and photosensitive recording material

    Legal Events

    Date Code Title Description
    PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

    Free format text: ORIGINAL CODE: 0009012

    AK Designated contracting states

    Kind code of ref document: A1

    Designated state(s): CH DE ES FR GB IT LI

    AX Request for extension of the european patent

    Free format text: AL;LT;LV;MK;RO;SI

    17P Request for examination filed

    Effective date: 19990610

    AKX Designation fees paid

    Free format text: CH DE ES FR GB IT LI

    17Q First examination report despatched

    Effective date: 20010712

    STAA Information on the status of an ep patent application or granted ep patent

    Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

    18D Application deemed to be withdrawn

    Effective date: 20011123